4.1 Review

The impact of preeclampsia on gene expression at the maternal-fetal interface

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.preghy.2010.12.001

Keywords

Placenta; Maternal-fetal interface; Basal plate; Preeclampsia

Funding

  1. NIH Grants [5K12HD00849, 2K12HD001271, R01 HD60723]
  2. General Clinical Research Center at San Francisco General Hospital [5-MO1-RR 00083]
  3. University of California, San Francisco, National Heart, Lung and Blood Institute Shared Microarray Facility [HL 072301]
  4. American Board of Obstetrics and Gynecology/American Association of Obstetricians and Gynecologists Foundation
  5. [R01 HL 64597]
  6. [R01 HD 30367]
  7. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [K12HD001271, P01HD030367, K12HD000849, R01HD060723] Funding Source: NIH RePORTER
  8. NATIONAL CENTER FOR RESEARCH RESOURCES [M01RR000833, M01RR000083] Funding Source: NIH RePORTER
  9. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL064597, R01HL072301] Funding Source: NIH RePORTER

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Preeclamp sia (PE) impacts 8 million mother-infant pairs worldwide each year. This human pregnancy-specific disease characterized by hypertension and proteinuria accounts for significant maternal and neonatal morbidity and mortality. The current theory of the pathogenesis of PE as reviewed by Dr. Christopher Redman and Dr. Ian Sargent is thought to occur as a 2-stage process with poor placentation in the first half of pregnancy resulting in the maternal response in the second half of pregnancy. Our studies have focused on understanding the placental contribution to this serious disease by examining the gene expression profile of the deciduas basalis or basal plate, the region of the placenta involved in the poor placentation''. In this review we present summaries of our microarray datasets both of normal placentation and those of gene expression changes resulting in the context of PE. Additionally, we have taken this opportunity to combine the datasets to provide a more comprehensive view of this region of the placenta. As defects in the basal plate are, in part, at the root of the disease process, we believe that understanding the pathobiology that occurs in this region will increase our ability to alter the development and/or course of PE. (C) 2010 International Society for the Study of Hypertension in Pregnancy. Published by Elsevier B.V. All rights reserved.

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